Devinylation of N-vinylpyrroles using mercury (II) acetate
EY Schmidt, AM Vasil'tsov, NV Zorina…
Index: Schmidt; Vasil'Tsov; Zorina; Ivanov; Mikhaleva; Trofimov Chemistry of Heterocyclic Compounds, 2012 , vol. 47, # 10 p. 1300 - 1303
Full Text: HTML
Citation Number: 5
Abstract
An N-vinyl group is one of the efficient and atom-economic groups for the protection of the NH-function in azoles [1]. Its removal is carried out by different methods: oxidation (KMnO4 [2, 3] or ozonolysis [4, 5]), acid hydrolysis [6-8], or acetomercuration and subsequent treatment with NaBH4 [6-13]. The synthetic use of pyrrole series compounds is limited by the comparatively small set of available NH-pyrroles since their syntheses are generally ...
Related Articles:
[Boukou-Poba, Jean-Paul; Farnier, Michel; Guilard, Roger Canadian Journal of Chemistry, 1981 , vol. 59, p. 2962 - 2967]
[Zeng, Jing; Bai, Yaguang; Cai, Shuting; Ma, Jimei; Liu, Xue-Wei Chemical Communications, 2011 , vol. 47, # 48 p. 12855 - 12857]
[Padwa, Albert; Stengel, Thomas Tetrahedron Letters, 2004 , vol. 45, # 31 p. 5991 - 5993]
[Pale-Grosdemange, Catherine; Chuche, Josselin Tetrahedron, 1989 , vol. 45, # 11 p. 3397 - 3414]
[Mikhaleva, Al'bina I.; Zaitsev, Alexey B.; Ivanov, Andrey V.; Schmidt, Elena Yu.; Vasil'tsov, Alexander M.; Trofimov, Boris A. Tetrahedron Letters, 2006 , vol. 47, # 22 p. 3693 - 3696]